Search results for "Nonmammalian"

showing 10 items of 127 documents

An acid extract from dissociation medium of sea urchin embryos, induces mesenchyme differentiation

1992

Abstract When material extracted by 1 M acetic acid from the dissociation medium of sea urchin embryos is added at low concentrations to isolated primary mesenchyme cells, it induces skeletogenesis. The same material added to dissociated blastula cells, or to embryos at the blastula stage, stimulates skeleton formation and pigment cell differentiation. On dissociated cells, it also increases cell reaggregation, thymidine incorporation and survival. On embryos, it induces exogastrulation and appearence of extraembryonic pigment cells. The activity of the extract is resistant to raised temperatures and partially to tryptic digestion but is abolished by trypsin treatment followed by heating. T…

Embryo Nonmammaliananimal structuresMesenchymeCellular differentiationUltrafiltrationBiologyMorulaPigment cell differentiationMesodermbiology.animalBotanymedicineAnimalsGrowth SubstancesSea urchinConnective Tissue CellsEmbryonic InductionTissue ExtractsEmbryogenesisCell DifferentiationEmbryoGastrulaCell BiologyHydrogen-Ion ConcentrationBlastulaTrypsinCell biologyBlastocystmedicine.anatomical_structureConnective TissueSea Urchinsembryonic structuresChromatography Liquidmedicine.drugCell Biology International Reports
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The p21-activated kinase Mbt is a component of the apical protein complex in central brain neuroblasts and controls cell proliferation

2013

The final size of the central nervous system is determined by precisely controlled generation, proliferation and death of neural stem cells. We show here that the Drosophila PAK protein Mushroom bodies tiny (Mbt) is expressed in central brain progenitor cells (neuroblasts) and becomes enriched to the apical cortex of neuroblasts in a cell cycle- and Cdc42-dependent manner. Using mushroom body neuroblasts as a model system, we demonstrate that in the absence of Mbt function, neuroblasts and their progeny are correctly specified and are able to generate different neuron subclasses as in the wild type, but are impaired in their proliferation activity throughout development. In general, loss of…

Embryo Nonmammaliananimal structuresMitosisApoptosisCell CountSpindle ApparatusBiologyNeural Stem CellsNeuroblastGTP-Binding ProteinsTubulinCell polarityAnimalsDrosophila ProteinsProgenitor cellMolecular BiologyMitosisCell ProliferationCell SizeBinding SitesApical cortexAsymmetric Cell DivisionfungiBrainCell PolarityGene Expression Regulation DevelopmentalNeural stem cellCell biologyEnzyme ActivationActin CytoskeletonPhenotypenervous systemLarvaMultiprotein Complexesembryonic structuresMushroom bodiesDrosophilaProtein KinasesGanglion mother cellDevelopmental BiologyDevelopment
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The RNA-binding protein ELAV regulates Hox RNA processing, expression and function within the Drosophila nervous system

2014

The regulated head-to-tail expression of Hox genes provides a coordinate system for the activation of specific programmes of cell differentiation according to axial level. Recent work indicates that Hox expression can be regulated via RNA processing but the underlying mechanisms and biological significance of this form of regulation remain poorly understood. Here we explore these issues within the developing Drosophila central nervous system (CNS). We show that the pan-neural RNA-binding protein (RBP) ELAV (Hu antigen) regulates the RNA processing patterns of the Hox gene Ultrabithorax (Ubx) within the embryonic CNS. Using a combination of biochemical, genetic and imaging approaches we demo…

Embryo Nonmammaliananimal structuresNeurogenesisRNA-binding proteinCellular differentiationMolecular Sequence DataRNA-binding proteinBiologyAntennapediaNervous SystemMorphogenesisAnimalsDrosophila ProteinsRNA Processing Post-TranscriptionalELAV/HuHox geneMolecular BiologyTranscription factorPhylogenyResearch ArticlesUltrabithoraxHomeodomain ProteinsAlternative polyadenylation (APA)GeneticsBase SequenceAlternative splicingGenes HomeoboxGene Expression Regulation DevelopmentalSegment-specific apoptosisHoxCell biologyDrosophila melanogasterELAV ProteinsRNA processingCentral nervous systemembryonic structuresDrosophilaDrosophila ProteinTranscription FactorsAlternative splicingDevelopmental BiologyDevelopment
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Constitutive Promoter Occupancy by the MBF-1 Activator and Chromatin Modification of the Developmental Regulated Sea Urchin α-H2A Histone Gene

2007

The tandemly repeated sea urchin alpha-histone genes are developmentally regulated. These genes are transcribed up to the early blastula stage and permanently silenced as the embryos approach gastrulation. As previously described, expression of the alpha-H2A gene depends on the binding of the MBF-1 activator to the 5' enhancer, while down-regulation relies on the functional interaction between the 3' sns 5 insulator and the GA repeats located upstream of the enhancer. As persistent MBF-1 binding and enhancer activity are detected in gastrula embryos, we have studied the molecular mechanisms that prevent the bound MBF-1 from trans-activating the H2A promoter at this stage of development. Her…

Embryo Nonmammaliananimal structuresRestriction MappingMBF-1Down-RegulationEnhancer RNAschromatin immunoprecipitationBiologyHistone DeacetylasesactivatorHistonesHistone H3Histone H1Structural BiologyHistone H2AHistone methylationAnimalsNucleosomeHistone codenucleosome phasingPromoter Regions GeneticEnhancerBase PairingMolecular Biologyhistone modificationsGene Expression Regulation DevelopmentalGastrulaMolecular biologyChromatinNucleosomesRepressor ProteinsMutagenesis InsertionalEnhancer Elements GeneticSea Urchinsembryonic structuresTrans-ActivatorsCalmodulin-Binding ProteinsInsulator Elementssea urchin histone geneProtein Processing Post-TranslationalProtein BindingJournal of Molecular Biology
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EGTA treatment causes the synthesis of heat shock proteins in sea urchin embryos.

2000

Paracentrotus lividus embryos, at post-blastular stage, when subjected to a rise in temperature from physiologic (20 degrees C) to 31 degrees C, synthesize a large group of heat shock proteins (hsps), and show a severe inhibition of bulk protein synthesis. We show, by mono- and two-dimensional electrophoresis, that also EGTA (ethylene glycol-bis[beta-aminoethyl ether] tetraacetic acid) treatment induces in sea urchin embryos both marked inhibition of bulk protein synthesis and the synthesis of the entire set of hsps. Furthermore, EGTA-treated sea urchin embryos are able to survive at a temperature otherwise lethal (35 degrees C) becoming thermotolerant. Because incubation with a different c…

Embryo NonmammalianbiologyEthylenediaminetetraacetic acidbiology.organism_classificationParacentrotus lividuschemistry.chemical_compoundEGTAchemistryBiochemistrybiology.animalHeat shock proteinSea UrchinsProtein biosynthesisBiophysicsAnimalsChelationElectrophoresis Gel Two-DimensionalMolecular BiologySea urchinIncubationEgtazic AcidEdetic AcidHeat-Shock ProteinsChelating AgentsMolecular cell biology research communications : MCBRC
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Cadmium induces an apoptotic response in sea urchin embryos.

2007

Cadmium is a heavy metal toxic for living organisms even at low concentrations. It does not have any biological role, and since it is a permanent metal ion, it is accumulated by many organisms. In the present paper we have studied the apoptotic effects of continuous exposure to subacute/sublethal cadmium concentrations on a model system: Paracentrotus lividus embryos. We demonstrated, by atomic absorption spectrometry, that the intracellular amount of metal increased during exposure time. We found, using terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay, that long treatments with cadmium triggered a severe DNA fragmentation. We demonstrated, by immunocytochemistry …

Embryo NonmammaliancadmiumImmunocytochemistrychemistry.chemical_elementWestern blotApoptosisDNA FragmentationEmbryo developmentCleavage (embryo)BiochemistryGel electrophoresiParacentrotus lividusIn Situ Nick-End LabelingIn Situ Nick-End LabelingAnimalssea urchin embryoCadmiumbiologyCaspase 3Stress proteinMicrofilament ProteinsCell BiologyOriginal Articlesbiology.organism_classificationMolecular biologyLaminschemistryApoptosisSea UrchinsDNA fragmentationCarrier ProteinsIntracellular
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The serosa of Manduca sexta (Insecta, Lepidoptera): ontogeny, secretory activity, structural changes, and functional considerations

2001

In Manduca sexta, the blastoderm forms successively and becomes immediately cellularized as the cleavage energids reach the surface of the oocyte. Presumptive serosal cells are large and contain 2 or 4 large polyploid nuclei; presumptive embryonic cells are small and mononuclear. All parts of the blastoderm participate in the uptake and digestion of yolk material. About 10 h post-oviposition, the blastoderm breaks at the amnioserosal fold and the extraembryonic part closes above the germ band and constitutes the serosa (12 h post-oviposition, i.e. 10% development completed). At once, the serosa starts to secrete a cuticle consisting of an epi- and a lamellated endocuticle. Detachment of the…

Embryo Nonmammalianfood.ingredientApolysisBiologysymbols.namesakefoodManducaYolkLipid dropletparasitic diseasesAnimalsYolk SacVesiclefungiEmbryogenesisCell BiologyGeneral MedicineAnatomyGolgi apparatusbiology.organism_classificationCell biologyMicroscopy ElectronManduca sextaOocytessymbolsInsect ProteinsBlastodermDevelopmental BiologyTissue and Cell
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Highly restricted expression at the ectoderm–endoderm boundary of PIHbox 9, a sea urchin homeobox gene related to the human HB9 gene

1998

Abstract Characterisation of a sea urchin (P. lividus) homeobox gene PIHbox 9 is reported. The homeodomain of PIHbox9 is 95% identical to the homeodomain of the human HB9 gene, indicating that the two genes are highly related. Temporal expression analysis during sea urchin embryogenesis showed an absence of transcripts at early cleavage stages. At late gastrula stage, transcripts were barely detectable and reached the highest abundance at prism/early pluteus stages. By whole mount in situ hybridisation we observed a highly restricted expression in a few cells of the ectoderm–endoderm boundary of embryos at the prism stage. At pluteus stages, expression of PIHbox 9 was confined around the an…

EmbryologyEmbryo Nonmammaliananimal structuresEctodermParacentrotus lividusbiology.animalEctodermmedicineAnimalsPluteusSea urchinIn Situ HybridizationHomeodomain ProteinsGeneticsbiologyEndodermEmbryogenesisGene Expression Regulation DevelopmentalGastrulabiology.organism_classificationCell biologyGastrulationmedicine.anatomical_structureSea Urchinsembryonic structuresHomeoboxEndodermTranscription FactorsDevelopmental BiologyMechanisms of Development
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A temperature-sensitive brain tumor suppressor mutation of Drosophila melanogaster: Developmental studies and molecular localization of the gene

1993

The recessive-lethal, temperature-sensitive (ts) mutation of the tumor suppressor gene lethal(3)malignant brain tumor (l(3)mbt) causes in a single step the malignant transformation of the adult optic neuroblasts and ganglion mother cells in the larval brain at the restrictive temperature of 29 degrees C. The transformed cells are differentiation-incompetent and grow autonomously in a lethal and invasive fashion in situ in the brain as well as after transplantation in vivo into wild-type adult hosts. The imaginal discs show epithelial overgrowth. At the permissive temperature of 22 degrees C development is completely normal. The ts-period of gene activity responsible for 100% brain tumor sup…

EmbryologyHot TemperatureTumor suppressor geneBiologymedicine.disease_causeMalignant transformationmedicineAnimalsGenes Tumor SuppressorGeneSuppressor mutationGeneticsMutationBrain NeoplasmsStem CellsOptic Lobe NonmammalianChromosome Mappingbiology.organism_classificationCell biologyTransplantationImaginal discDrosophila melanogasterGangliaGenes LethalDrosophila melanogasterDevelopmental BiologyMechanisms of Development
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saliva, a new Drosophila gene expressed in the embryonic salivary glands with homologues in plants and vertebrates.

1998

saliva (slv) transcription begins at the salivary gland placodes and continues on throughout development as salivary glands invaginate and reach their final location and morphology. saliva is located cytogenetically in 76A/B, and encodes a 226-amino-acid protein with four hydrophobic domains. A Northern blot detects a 1.6-kb transcript throughout development. Database similarity searches reveal homology to proteins from Caenorhabditis, Lilium, Medicago and mouse.

EmbryologySalivaDNA ComplementaryEmbryo NonmammalianDNA PlantMolecular Sequence DataGenes InsectGenes PlantHomology (biology)Salivary Glandsstomatognathic systemmedicineAnimalsDrosophila ProteinsNorthern blotAmino Acid SequenceSalivary Proteins and PeptidesGeneIn Situ HybridizationbiologySalivary glandSequence Homology Amino AcidGene Expression Regulation DevelopmentalSequence Analysis DNAPlantsbiology.organism_classificationMolecular biologyCaenorhabditismedicine.anatomical_structureDrosophila melanogasterVertebratesDrosophila melanogasterSequence AlignmentDrosophila ProteinDevelopmental BiologyMechanisms of development
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